Evidence map›Paper›PMID 29705331›Full record

ArticleDevelopmental biology2018

Disparate levels of beta-catenin activity determine nephron progenitor cell fate.

Harini Ramalingam, Alicia R Fessler, Amrita Das, M Todd Valerius, Jeannine Basta, Lynn Robbins, Aaron C Brown, Leif Oxburgh, Andrew P McMahon, Michael Rauchman and 1 more

Open access · greenAbstract read
In one paragraph

Article in Developmental biology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
2.0field-weighted citation impact, top 13% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

31 citing papers in PubMed, 46 citations in OpenAlex.

  1. Epigenetic regulation of kidney development.Nature reviews. Nephrology · 2026
    Review
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  5. Measurement of adhesion and traction of cells at high yield reveals an energetic ratchet operating during nephron condensation.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
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  10. Review
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  15. Principles of human and mouse nephron development.Nature reviews. Nephrology · 2022
    Review
  16. Review
  17. Article
  18. Article
  19. A methionine-Mettl3-NCell metabolism · 2021
    Article
  20. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors at 6 institutions in 1 country.

Harini RamalingamDepartments of Internal Medicine (Nephrology), University of Texas Southwestern Medical Center, 5323 Harry Hines Blvd., Dallas, TX 75390-9148, USA; Molecular Biology, University of Texas Southwestern Medical Center, 5323 Harry Hines Blvd., Dallas, TX 75390-9148, USA.
Alicia R FesslerDepartments of Internal Medicine (Nephrology), University of Texas Southwestern Medical Center, 5323 Harry Hines Blvd., Dallas, TX 75390-9148, USA; Molecular Biology, University of Texas Southwestern Medical Center, 5323 Harry Hines Blvd., Dallas, TX 75390-9148, USA.
Amrita DasDepartments of Internal Medicine (Nephrology), University of Texas Southwestern Medical Center, 5323 Harry Hines Blvd., Dallas, TX 75390-9148, USA; Molecular Biology, University of Texas Southwestern Medical Center, 5323 Harry Hines Blvd., Dallas, TX 75390-9148, USA.
M Todd ValeriusRenal Division, Brigham and Women's Hospital, Department of Medicine, Harvard Medical School, Boston, MA 02115, USA; Harvard Stem Cell Institute, Cambridge, MA 02138, USA.
Jeannine BastaDepartment of Internal Medicine, Saint Louis University, St Louis, MO 63104, USA; Department of Biochemistry and Molecular Biology, Saint Louis University, St Louis, MO 63104, USA; VA St. Louis Health Care System, John Cochran Division, St Louis, MO 63106, USA.
Lynn RobbinsDepartment of Internal Medicine, Saint Louis University, St Louis, MO 63104, USA; Department of Biochemistry and Molecular Biology, Saint Louis University, St Louis, MO 63104, USA; VA St. Louis Health Care System, John Cochran Division, St Louis, MO 63106, USA.
Aaron C BrownCenter for Molecular Medicine, Maine Medical Center Research Institute, Scarborough, ME 04074, USA.
Leif OxburghCenter for Molecular Medicine, Maine Medical Center Research Institute, Scarborough, ME 04074, USA.
Andrew P McMahonDepartment of Stem Cell Biology and Regenerative Medicine, W.M. Keck School of Medicine of the University of Southern California,1425 San Pablo Street, Los Angeles, CA 90033, USA; Eli and Edythe Broad-CIRM Center for Regenerative Medicine and Stem Cell Research, W.M. Keck School of Medicine of the University of Southern California, 1425 San Pablo Street, Los Angeles, CA 90033, USA.
Michael RauchmanDepartment of Internal Medicine, Saint Louis University, St Louis, MO 63104, USA; Department of Biochemistry and Molecular Biology, Saint Louis University, St Louis, MO 63104, USA; VA St. Louis Health Care System, John Cochran Division, St Louis, MO 63106, USA.
Thomas J CarrollDepartments of Internal Medicine (Nephrology), University of Texas Southwestern Medical Center, 5323 Harry Hines Blvd., Dallas, TX 75390-9148, USA; Molecular Biology, University of Texas Southwestern Medical Center, 5323 Harry Hines Blvd., Dallas, TX 75390-9148, USA. Electronic address: thomas.carroll@utsouthwestern.edu.
The University of Texas Southwestern Medical Center · USVA St. Louis Health Care System · USMaine Medical Center · USBrigham and Women's Hospital · USSouthwestern Medical Center · USUniversity of Southern California · US

Funding

UT Southwestern O'Brien Kidney Research Core CenterP30DK079328 · NIDDK · UT SOUTHWESTERN MEDICAL CENTER · PI MOE, ORSON W · 2007 to 2021
$16.9M
Cell Interactions in Development of the Mammalian KidneyR37DK054364 · NIDDK · UNIVERSITY OF SOUTHERN CALIFORNIA · PI MCMAHON, ANDREW P. · 2008 to 2017
$7.0M
Engineering erythropoietin-producing cellsR24DK106743 · NIDDK · ROGOSIN INSTITUTE · PI CARROLL, THOMAS JOSEPH, CLEAVER, ONDINE B · 2015 to 2019
$7.0M
CELL INTERACTIONS IN DEVELOPMENT OF THE MAMMALIAN KIDNEYR01DK054364 · NIDDK · UNIVERSITY OF SOUTHERN CALIFORNIA · PI MCMAHON, ANDREW P. · 1998 to 2022
$6.9M
Defining the progenitor cell niche of the developing kidneyR01DK078161 · NIDDK · MAINEHEALTH · PI OXBURGH, LEIF · 2008 to 2016
$3.4M
The role of Wnt signaling in kidney tubule formationR01DK080004 · NIDDK · UT SOUTHWESTERN MEDICAL CENTER · PI CARROLL, THOMAS JOSEPH · 2008 to 2012
$1.6M
Interactions between the stroma and progenitor cells during kidney developmentR01DK095057 · NIDDK · UT SOUTHWESTERN MEDICAL CENTER · PI CARROLL, THOMAS JOSEPH · 2013 to 2016
$1.4M
Delineating a role for non-canonical wnt signaling in PKDR01DK090127 · NIDDK · UT SOUTHWESTERN MEDICAL CENTER · PI CARROLL, THOMAS JOSEPH · 2013 to 2016
$1.4M
Regulation of Nephron Progenitor Cell Self-Renewal and DifferentiationR01DK098563 · NIDDK · WASHINGTON UNIVERSITY · PI RAUCHMAN, MICHAEL I · 2014 to 2017
$1.3M
Molecular Regulation of Nephron FormationF32DK060319 · NIDDK · HARVARD UNIVERSITY · PI VALERIUS, MICHAEL T · 2001 to 2003
$118k
NIDDK NIH HHS F32 DK060319NIDDK NIH HHS P30 DK079328NIDDK NIH HHS R01 DK054364NIDDK NIH HHS R01 DK078161NIDDK NIH HHS R01 DK080004NIDDK NIH HHS R01 DK090127NIDDK NIH HHS R01 DK095057NIDDK NIH HHS R01 DK098563NIDDK NIH HHS R24 DK106743NIDDK NIH HHS R37 DK054364
6 · The paper itself

Abstract

Formation of a functional kidney depends on the balance between renewal and differentiation of nephron progenitors. Failure to sustain this balance can lead to kidney failure or stem cell tumors. For nearly 60 years, we have known that signals from an epithelial structure known as the ureteric bud were essential for maintaining this balance. More recently it was discovered that one molecule, Wnt9b, was necessary for both renewal and differentiation of the nephron progenitor cells. How one ligand signaling through one transcription factor promoted two seemingly contradictory cellular processes was unclear. In this study, we show that Wnt9b/beta-catenin signaling alone is sufficient to promote both renewal and differentiation. Moreover, we show that discrete levels of beta-catenin can promote these two disparate fates, with low levels fostering progenitor renewal and high levels driving differentiation. These results provide insight into how Wnt9b regulates distinct target genes that balance nephron progenitor renewal and differentiation.

Indexed as

Animalsbeta CateninCell DifferentiationGene Expression RegulationKidneyMiceMice, Inbred C57BLMice, TransgenicNephronsSignal TransductionStem CellsTranscription FactorsWnt ProteinsWnt Signaling Pathwaybeta CateninTranscription FactorsWnt Proteins

Identifiers

PMID29705331
PMCPMC5988999
OpenAlexW2802657547

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.